SUPERFICIAL THROMBOPHLEBITIS .1. PRIMARY HYPERCOAGULABLE STATES

被引:43
作者
SAMLASKA, CP
JAMES, WD
机构
[1] Dermatology Service, Walter Reed Army Medical Center, Washington, District of Columbia
关键词
D O I
10.1016/0190-9622(90)70139-9
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
This review concentrates on those disorders in which superficial thrombophlebitis can be a significant or presenting clinical sign. Primary hypercoagulable states are those conditions associated with an increased risk of thrombosis caused by a specific measurable defect in the proteins of coagulation and/or fibrinolytic systems. These disorders are frequently inherited and include deficiencies of antithrombin III, heparin cofactor 2, protein C, protein S, abnormal fibrinolytic activity, dysfibrinogenemia, and Hageman trait. Patients with a lupus anticoagulant and anticardiolipin antibody syndrome with thrombotic episodes are also considered to have a primary hypercoagulable state. The physiology, pathophysiology, clinical characteristics, and treatment of primary hypercoagulable states are reviewed. © 1990, American Academy of Dermatology, Inc.. All rights reserved.
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收藏
页码:975 / 989
页数:15
相关论文
共 172 条
[91]  
LIJNEN HR, 1984, THROMB HAEMOSTASIS, V51, P108
[92]  
LIU C Y, 1979, Thrombosis and Haemostasis, V42, P79
[93]  
LIU CY, 1979, J BIOL CHEM, V254, P421
[94]  
LIU Y, 1988, THROMB HAEMOSTASIS, V59, P49
[95]  
LODI S, 1984, SCAND J HAEMATOL, V33, P80
[96]  
LOTTENBERG R, 1983, CLIN RES, V31, pA318
[97]  
MANNUCCI PM, 1982, LANCET, V2, P463
[98]   TREATMENT OF CONGENITAL ANTITHROMBIN-III DEFICIENCY WITH CONCENTRATES [J].
MANNUCCI, PM ;
BOYER, C ;
WOLF, M ;
TRIPODI, A ;
LARRIEU, MJ .
BRITISH JOURNAL OF HAEMATOLOGY, 1982, 50 (03) :531-535
[99]  
MARCINIAK E, 1985, BLOOD, V65, P15
[100]   DIAGNOSIS AND TREATMENT OF HOMOZYGOUS PROTEIN-C DEFICIENCY [J].
MARLAR, RA ;
MONTGOMERY, RR ;
BROEKMANS, AW .
JOURNAL OF PEDIATRICS, 1989, 114 (04) :528-534